LDH info

Canonical Allele Identifier: CA369856095
Gene: KCNH2 HGNC NCBI

Identifiers and link-outs to other resources

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.150950231G>T , CM000669.2:g.150950231G>T GRCh38
NC_000007.13:g.150647319G>T , CM000669.1:g.150647319G>T GRCh37
NC_000007.12:g.150278252G>T NCBI36
NG_008916.1:g.32696C>A , LRG_288:g.32696C>A

Transcript Alleles

HGVS Amino-acid change
NM_000238.3:c.2335C>A , LRG_288t1:c.2335C>A NP_000229.1:p.Leu779Met
NM_001204798.1:c.1315C>A VV NP_001191727.1:p.Leu439Met
NM_172056.2:c.2335C>A , LRG_288t2:c.2335C>A NP_742053.1:p.Leu779Met
NM_172057.2:c.1315C>A , LRG_288t3:c.1315C>A NP_742054.1:p.Leu439Met
XM_011516185.1:c.2035C>A XP_011514487.1:p.Leu679Met
XM_011516186.1:c.2335C>A XP_011514488.1:p.Leu779Met
XM_011516185.2:c.2035C>A XP_011514487.1:p.Leu679Met
XM_011516186.3:c.2335C>A XP_011514488.1:p.Leu779Met
XM_017012195.1:c.2185C>A XP_016867684.1:p.Leu729Met
XM_017012196.1:c.2158C>A XP_016867685.1:p.Leu720Met
NM_000238.4:c.2335C>A VV MANE Preferred NP_000229.1:p.Leu779Met
NM_001204798.2:c.1315C>A VV NP_001191727.1:p.Leu439Met
ENST00000262186.9:c.2335C>A ENSP00000262186.5:p.Leu779Met
ENST00000330883.8:c.1315C>A ENSP00000328531.4:p.Leu439Met
ENST00000430723.4:c.1987C>A ENSP00000387657.4:p.Leu663Met
ENST00000461280.1:n.1622C>A
ENST00000473610.5:n.1967C>A
ENST00000532957.5:n.2558C>A